A highly versatile automatized setup for quantitative measurements of PHIP enhancements Научная публикация
| Журнал |
Journal of Magnetic Resonance
ISSN: 1090-7807 |
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| Вых. Данные | Год: 2017, Том: 285, Страницы: 26-36 Страниц : 11 DOI: 10.1016/j.jmr.2017.10.007 | ||||||
| Ключевые слова | Hyperpolarization, Parahydrogen Induced Polarization, Kinetics, Gas-dissolution | ||||||
| Авторы |
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| Организации |
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Реферат:
The design and application of a versatile and inexpensive experimental extension to NMR spectrometers is described that allows to carry out highly reproducible PHIP experiments directly in the NMR sample tube, i.e. under PASADENA condition, followed by the detection of the NMR spectra of hyperpolarized products with high spectral resolution. Employing this high resolution it is feasible to study kinetic processes in the solution with high accuracy. As a practical example the dissolution of hydrogen gas in the liquid and the PHIP kinetics during the hydrogenation reaction of Fmoc-O-propargyl-L-tyrosine in acetone-d6 are monitored. The timing of the setup is fully controlled by the pulse-programmer of the NMR spectrometer. By flushing with an inert gas it possible to efficiently quench the hydrogenation reaction in a controlled fashion and to detect the relaxation of hyperpolarization without a background reaction. The proposed design makes it possible to carry out PHIP experiments in an automatic mode and reliably determine the enhancement of polarized signals.
Библиографическая ссылка:
Kiryutin A.S.
, Sauer G.
, Hadjiali S.
, Yurkovskaya A.V.
, Breitzke H.
, Buntkowsky G.
A highly versatile automatized setup for quantitative measurements of PHIP enhancements
Journal of Magnetic Resonance. 2017. V.285. P.26-36. DOI: 10.1016/j.jmr.2017.10.007
A highly versatile automatized setup for quantitative measurements of PHIP enhancements
Journal of Magnetic Resonance. 2017. V.285. P.26-36. DOI: 10.1016/j.jmr.2017.10.007
Даты:
| Поступила в редакцию: | 18 авг. 2017 г. |
| Принята к публикации: | 14 окт. 2017 г. |
| Опубликована online: | 16 окт. 2017 г. |
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